The eQTL SMR results had been left out of the following repository due to an error https://zenodo.org/record/3518299 sQTL SMR results have also been uploaded to https://zenodo.org/record/3525070 ---------- sqlite version of these results are also available here https://github.com/abhiramrao/gtex_v8_GPMs ---------- The GTEx Consortium SMR results using eQTL and sQTLs from GTEx (release 8) # Data usage policy When using this data, you must acknowledge the source by citing the publication "Widespread dose-dependent effects of RNA expression and splicing on complex diseases and traits" (https://doi.org/10.1101/814350). # Disclaimer The data is provided "as is", and the authors assume no responsibility for errors or omissions. Th...
This is a normalized dataset from the original RNAseq dataset downloaded from Genotype-Tissue Expres...
The eQTL Catalogue is an open database of uniformly processed human molecular quantitative trait loc...
International audienceAlthough it is necessary to identify candidate genes, there is actually no wel...
# Data usage policy When using this data, you must acknowledge the source by citing the publication...
Cohort: cohort of the eQTL study, probeID: ID of the probe used in respective cohorts for gene of in...
# harmonized and imputed GWAS summary statistics * `harmonized_imputed_gwas.tar` contains 114 pu...
# Introduction Sample data for mixQTL (https://github.com/liangyy/mixqtl). Data is derived from th...
sQTL catalog generated by sqtlseeker2-nf in the GTEx dataset, as described in the publication Identi...
This version of the source code reflects analyses included in the peer-reviewed manuscript "Impact o...
# GWAS summary statistics imputation, integration with PrediXcan MASHR-M The file `sample_data.t...
Genome-wide association studies (GWASs) have shown a large number of genetic variants to be associat...
The resources generated by the GTEx consortium offer unprecedented opportunities to advance our unde...
eQTL summary statistics and GWAS colocalization posterior probabilities from eQTL calling in an admi...
The tables were used in the papers: Rouhana*, Wang* et al., ECLIPSER: identifying causal cell types ...
Cohort: cohort of the eQTL study, probeID: ID of the probe used in respective cohorts for gene of in...
This is a normalized dataset from the original RNAseq dataset downloaded from Genotype-Tissue Expres...
The eQTL Catalogue is an open database of uniformly processed human molecular quantitative trait loc...
International audienceAlthough it is necessary to identify candidate genes, there is actually no wel...
# Data usage policy When using this data, you must acknowledge the source by citing the publication...
Cohort: cohort of the eQTL study, probeID: ID of the probe used in respective cohorts for gene of in...
# harmonized and imputed GWAS summary statistics * `harmonized_imputed_gwas.tar` contains 114 pu...
# Introduction Sample data for mixQTL (https://github.com/liangyy/mixqtl). Data is derived from th...
sQTL catalog generated by sqtlseeker2-nf in the GTEx dataset, as described in the publication Identi...
This version of the source code reflects analyses included in the peer-reviewed manuscript "Impact o...
# GWAS summary statistics imputation, integration with PrediXcan MASHR-M The file `sample_data.t...
Genome-wide association studies (GWASs) have shown a large number of genetic variants to be associat...
The resources generated by the GTEx consortium offer unprecedented opportunities to advance our unde...
eQTL summary statistics and GWAS colocalization posterior probabilities from eQTL calling in an admi...
The tables were used in the papers: Rouhana*, Wang* et al., ECLIPSER: identifying causal cell types ...
Cohort: cohort of the eQTL study, probeID: ID of the probe used in respective cohorts for gene of in...
This is a normalized dataset from the original RNAseq dataset downloaded from Genotype-Tissue Expres...
The eQTL Catalogue is an open database of uniformly processed human molecular quantitative trait loc...
International audienceAlthough it is necessary to identify candidate genes, there is actually no wel...